TY - JOUR
T1 - Recommendations for evaluation and management of bone disease in HIV
AU - Brown, Todd T.
AU - Hoy, Jennifer
AU - Borderi, Marco
AU - Guaraldi, Giovanni
AU - Renjifo, Boris
AU - Vescini, Fabio
AU - Yin, Michael T.
AU - Powderly, William G.
N1 - Funding Information:
Potential conflicts of interest. T. T. B. has served as a consultant to Abb-Vie, ViiV Healthcare, Merck, Gilead, Theratechnologies, and EMD-Serono. J. H.’s institution has received funding from Gilead Sciences, ViiV Healthcare, Merck Sharp & Dohme for her participation in advisory boards, and from AbbVie for her participation in OREP. M. B. has participated in programs supported by AbbVie. G. G. has received consulting fees and honorarium from AbbVie, has served on advisory boards for Gilead and Merck, and has served as a speaker for AbbVie, Gilead, Bristol-Myers Squibb (BMS), ViiV Healthcare, and Merck. B. R. is an AbbVie employee and may hold Abbott or AbbVie stocks or options. F. V. has received grants for scientific speeches by Gilead Sciences, AbbVie, ViiV Healthcare, BMS, Abiogen Pharma, Merck Sharp & Dohme, Amgen, Lilly Pharmaceuticals, and SPA Pharma. M. T. Y. has served as a consultant to AbbVie and Gilead. W. G. P. has received consultancy fees from AbbVie, Tibotec-Jans-sen, Merck, Calimmune, and BMS and speaker fees from Janssen.
Funding Information:
Financial support. This work was supported by AbbVie, who selected the invited participants to OREP and provided honoraria for the participants’ attendance at the meetings. No payments were made to the authors for the development of this manuscript. Susan Cheer and Lucy Hampson of Lucid Group, Buckinghamshire, UK, provided medical writing and editorial support to the authors in the development of this manuscript and this was supported by AbbVie.
Publisher Copyright:
© The Author 2015. Published by Oxford University Press on behalf of the Infectious Diseases Society of America.
PY - 2015/4/15
Y1 - 2015/4/15
N2 - Thirty-four human immunodeficiency virus (HIV) specialists from 16 countries contributed to this project, whose primary aim was to provide guidance on the screening, diagnosis, and monitoring of bone disease in HIV-infected patients. Four clinically important questions in bone disease management were identified, and recommendations, based on literature review and expert opinion, were agreed upon. Risk of fragility fracture should be assessed primarily using the Fracture Risk Assessment Tool (FRAX), without dual-energy X-ray absorptiometry (DXA), in all HIV-infected men aged 40-49 years and HIV-infected premenopausal women aged ≥ 40 years. DXA should be performed in men aged ≥ 50 years, postmenopausal women, patients with a history of fragility fracture, patients receiving chronic glucocorticoid treatment, and patients at high risk of falls. In resource-limited settings, FRAX without bone mineral density can be substituted for DXA. Guidelines for antiretroviral therapy should be followed; adjustment should avoid tenofovir disoproxil fumarate or boosted protease inhibitors in at-risk patients. Dietary and lifestyle management strategies for high-risk patients should be employed and antiosteoporosis treatment initiated.
AB - Thirty-four human immunodeficiency virus (HIV) specialists from 16 countries contributed to this project, whose primary aim was to provide guidance on the screening, diagnosis, and monitoring of bone disease in HIV-infected patients. Four clinically important questions in bone disease management were identified, and recommendations, based on literature review and expert opinion, were agreed upon. Risk of fragility fracture should be assessed primarily using the Fracture Risk Assessment Tool (FRAX), without dual-energy X-ray absorptiometry (DXA), in all HIV-infected men aged 40-49 years and HIV-infected premenopausal women aged ≥ 40 years. DXA should be performed in men aged ≥ 50 years, postmenopausal women, patients with a history of fragility fracture, patients receiving chronic glucocorticoid treatment, and patients at high risk of falls. In resource-limited settings, FRAX without bone mineral density can be substituted for DXA. Guidelines for antiretroviral therapy should be followed; adjustment should avoid tenofovir disoproxil fumarate or boosted protease inhibitors in at-risk patients. Dietary and lifestyle management strategies for high-risk patients should be employed and antiosteoporosis treatment initiated.
KW - bone disease
KW - fragility fracture
KW - human immunodeficiency virus
KW - osteoporosis
UR - http://www.scopus.com/inward/record.url?scp=84926633782&partnerID=8YFLogxK
U2 - 10.1093/cid/civ010
DO - 10.1093/cid/civ010
M3 - Article
C2 - 25609682
AN - SCOPUS:84926633782
SN - 1058-4838
VL - 60
SP - 1242
EP - 1251
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 8
ER -